Neurology Genetic Testing

Neurology Genetic Testing is a diagnostic tool used to identify inherited genetic mutations that affect the nervous system. It helps detect the genetic causes of neurological disorders such as epilepsy, muscular dystrophy, ataxia, Parkinson’s disease, and hereditary neuropathies. By analyzing an individual’s DNA, this testing can reveal mutations passed down through families, enabling early diagnosis, risk assessment, and personalized treatment plans. It is particularly useful when neurological symptoms are unexplained or when there’s a family history of neurological disease. Neurology genetic testing supports informed decision-making, aids in family planning, and may qualify patients for clinical trials or targeted therapies.

Why Choose This Neurology Genetic Testing?

Choosing neurology genetic testing provides critical insights into the underlying causes of unexplained neurological symptoms, enabling earlier and more accurate diagnoses. It helps identify inherited conditions that may not be detectable through traditional methods, guiding more effective, personalized treatment strategies. This testing also offers valuable information for family members, revealing potential hereditary risks and supporting proactive health management. With advances in precision medicine, genetic testing can connect patients to targeted therapies and clinical trials. Overall, it empowers patients and clinicians with knowledge that can improve outcomes, inform long-term care plans, and provide clarity in complex neurological cases.

When Is It Used?

When a patient shows persistent symptoms like seizures, tremors, or muscle weakness without a clear cause.
In cases where conditions such as epilepsy, dementia, or movement disorders appear at an unusually young age.
When there is a known history of inherited neurological conditions in the family.
To identify genetic causes in patients experiencing worsening cognitive or motor function over time.
For individuals at risk of inherited neurological diseases but not yet showing symptoms.
For couples concerned about passing on genetic neurological disorders to their children.

Who Should Consider Neurology Genetic Testing?

Neurology genetic testing is recommended for individuals experiencing unexplained or progressive neurological symptoms, especially when there is a known family history of similar disorders. It is also beneficial for those diagnosed with a neurological condition at a young age, or anyone planning a family who wants to assess the risk of passing on genetic conditions. This testing helps uncover inherited causes, enabling early intervention, tailored treatment, and informed family decisions.

You should consider this test if:

Individuals with a family history of neurological disorders (e.g., ALS, Huntington’s disease).
Patients with early-onset epilepsy, dementia, or Parkinsonism.
Children with developmental delays, hypotonia, or intellectual disabilities.
People with unexplained muscle weakness, neuropathy, or movement disorders.
Couples seeking genetic counseling for family planning.
Patients with progressive or treatment-resistant neurological symptoms.

How We Work

How is the Test Performed?

Our Services

Just a few of the many health issues we screen for

Epilepsy

A neurological disorder causing recurrent seizures due to abnormal brain electrical activity, often with genetic mutations influencing treatment and prognosis.

Parkinson’s Disease

A progressive movement disorder characterized by tremors, rigidity, and bradykinesia, sometimes caused by inherited gene mutations affecting dopamine-producing brain cells.

Huntington’s Disease

An inherited disorder causing progressive brain cell degeneration, leading to movement, cognitive, and psychiatric symptoms, caused by a specific gene mutation.

Ataxia

A disorder causing lack of muscle coordination and balance, often resulting from genetic mutations affecting cerebellar function or sensory pathways.

Multiple Sclerosis

An autoimmune disorder damaging the central nervous system’s myelin sheath, with genetic factors contributing to susceptibility and disease progression.

Muscular Dystrophy

A group of genetic diseases characterized by progressive muscle degeneration and weakness, caused by mutations affecting muscle protein production.

Who we Are

Why Choose Us?

State-of-the-Art Digital Lab Experience

Our fully integrated E-Lab platform offers online test ordering, real-time tracking, and secure digital reporting bringing convenience and control to both physicians and patients across the country.

Advanced Diagnostic Technology

From routine blood tests to complex genetic panels, we leverage cutting-edge platforms like NGS, PCR, and AI-powered analytics for maximum accuracy and clinical relevance.

Fast Turnaround, Local Support

With lab facilities based in Florida, we ensure faster processing times and direct access to our expert team. You get timely results backed by responsive, local customer support.

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